Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. GENERAL SUMMARY:Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research ...
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study complian...
Clinical Research Coordinators. Clinical Research Coordinators are responsible to coordinate and manage multiple studies. IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical researc...
Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Bachel...
Knowledge equivalent to that which normally would be acquired through a four year college degree program in a clinical field such as health or biological science and a minimum of one to three years of related and progressively more responsible or expansive work experience in clinical and/or research...
They will support Principal Investigators, Drs Rachel Marsh, Kate Fitzgerald, and David Pagliaccio, and the research team in the successful implementation of clinical research activities. CDNL is seeking a project coordinator to facilitate a clinical trial examining the use of a cognitive control tr...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
We are seeking a full-time Clinical Research Coordinator with a minimum of 1 year of clinical experience. Clinical Research Coordinators here at Revival Research Institute , should be genuinely respectful of diverse points-of-view and s...
We are seeking a Clinical Research Coordinator to join our team and contribute to a NIH-funded study on acute respiratory distress syndrome (ARDS) recovery. Conduct outpatient clinic research follow-up visits, including repeating questionnaires, measures of physical function, and phlebotomy. ...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study complian...
Barrington James is looking for Clinical Research Coordinators in multiple locations within Michigan to join our client. This is a 3-6 month contract opportunity, this is a great opportunity to build a professional relationship with the client and to grow into other positions within the Clinical Res...
Clinical Research Coordinator - Department of Pharmacy Practice. Clinical Research Coordinator - Department of Pharmacy Practice. POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data....
Clinical Research Coordinator I The CRC I will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Liaising with Laboratory team...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Assist study team with aspects of clinical research coordination including: identifying potential subjects, screening subjects, consenting and enrolling subjects, and collecting and managing patient and laboratory data for clinical research subjects. There is a need to move, transport, and position ...
Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field. Previous coordinator experience preferred. Department: Cancer Clinical & Trans...
Clinical Research Coordinator Responsibilities. Minimum 5+ years of directly related experience in clinical research and clinical trials is necessary. Will serve as the central administrative coordinator, facilitating communication across research teams, sponsors, and other stakeholders across the d...
The Clinical Research Coordinator (CRC) will play a vital role in supporting the Division of Nephrology's research activities within the Metabolic Bone Disease Unit. Working closely with the Principal Investigator (PI) and other research staff, you will be instrumental in collecting data and coordin...
Provide experienced Clinical Research Coordinator (CRC) support to the Clinical Trials Office (CTO) and Multidisciplinary Team (MDT) team. Clinical Research Professional or Association of Clinical Research Professionals (ACRP) required for a minimum of 12 months prior to assuming CRC IV role. Bachel...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Provide study coordinator/datamanagement/regulatory specialist support to the Clinical Trials Office (CTO). Assist multidisciplinary team in research activities. ...